Visitor Monitoring Drug Details: IMITREX
 
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Drug Details

Drug Name: IMITREX
FDA Application No: (NDA) 020132
Active Ingredient(s): SUMATRIPTAN SUCCINATE
Company: GLAXOSMITHKLINE
Original Approval or Tentative Approval Date: June 1, 1995
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
IMITREX SUMATRIPTAN SUCCINATEEQ 100MG BASETABLET; ORAL Prescription Yes None
IMITREX SUMATRIPTAN SUCCINATEEQ 25MG BASETABLET; ORAL Prescription No None
IMITREX SUMATRIPTAN SUCCINATEEQ 50MG BASETABLET; ORAL Prescription No None


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